CID 162904760

Details

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Internal ID bc9f04f7-0001-4c8b-a80d-4aeb6dab0b90
Taxonomy Organoheterocyclic compounds > Naphthopyrans
IUPAC Name
SMILES (Canonical) CCC(C)C(=O)OC1C(C2(C(CCC3(O2)CC(=O)OC3)(C4C1(C5(CCC4)CO5)COC(=O)C)C)C)OC(=O)C
SMILES (Isomeric) CCC(C)C(=O)OC1C(C2(C(CCC3(O2)CC(=O)OC3)(C4C1(C5(CCC4)CO5)COC(=O)C)C)C)OC(=O)C
InChI InChI=1S/C29H42O10/c1-7-17(2)24(33)38-23-22(37-19(4)31)26(6)25(5,11-12-27(39-26)13-21(32)35-14-27)20-9-8-10-28(15-36-28)29(20,23)16-34-18(3)30/h17,20,22-23H,7-16H2,1-6H3
InChI Key AQVZDJYNIRKSER-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C29H42O10
Molecular Weight 550.60 g/mol
Exact Mass 550.27779753 g/mol
Topological Polar Surface Area (TPSA) 127.00 Ų
XlogP 2.80
Atomic LogP (AlogP) 3.27
H-Bond Acceptor 10
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 162904760

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9635 96.35%
Caco-2 - 0.6391 63.91%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.7337 73.37%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8131 81.31%
OATP1B3 inhibitior + 0.9731 97.31%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior + 0.9785 97.85%
P-glycoprotein inhibitior + 0.7679 76.79%
P-glycoprotein substrate - 0.5625 56.25%
CYP3A4 substrate + 0.6689 66.89%
CYP2C9 substrate - 0.8095 80.95%
CYP2D6 substrate - 0.8590 85.90%
CYP3A4 inhibition - 0.8104 81.04%
CYP2C9 inhibition - 0.8558 85.58%
CYP2C19 inhibition - 0.7147 71.47%
CYP2D6 inhibition - 0.9402 94.02%
CYP1A2 inhibition - 0.8723 87.23%
CYP2C8 inhibition + 0.6457 64.57%
CYP inhibitory promiscuity - 0.8551 85.51%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5844 58.44%
Eye corrosion - 0.9848 98.48%
Eye irritation - 0.8862 88.62%
Skin irritation - 0.7163 71.63%
Skin corrosion - 0.9152 91.52%
Ames mutagenesis - 0.5864 58.64%
Human Ether-a-go-go-Related Gene inhibition + 0.6487 64.87%
Micronuclear - 0.5800 58.00%
Hepatotoxicity - 0.6474 64.74%
skin sensitisation - 0.8980 89.80%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.5540 55.40%
Acute Oral Toxicity (c) III 0.3967 39.67%
Estrogen receptor binding + 0.8615 86.15%
Androgen receptor binding + 0.7266 72.66%
Thyroid receptor binding + 0.5353 53.53%
Glucocorticoid receptor binding + 0.7880 78.80%
Aromatase binding + 0.7458 74.58%
PPAR gamma + 0.7166 71.66%
Honey bee toxicity - 0.7338 73.38%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6450 64.50%
Fish aquatic toxicity + 0.9704 97.04%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL2581 P07339 Cathepsin D 98.01% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.13% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.65% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.23% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.46% 96.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 94.18% 96.77%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.38% 97.09%
CHEMBL2782 P35610 Acyl coenzyme A:cholesterol acyltransferase 1 90.38% 91.65%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 89.25% 82.69%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 88.72% 95.17%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 88.40% 92.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.20% 95.56%
CHEMBL2996 Q05655 Protein kinase C delta 87.58% 97.79%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.17% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.71% 99.23%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 86.67% 95.71%
CHEMBL1293316 Q9HBX9 Relaxin receptor 1 86.04% 82.50%
CHEMBL340 P08684 Cytochrome P450 3A4 85.00% 91.19%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.92% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.62% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.47% 86.33%
CHEMBL5255 O00206 Toll-like receptor 4 82.95% 92.50%
CHEMBL2964 P36507 Dual specificity mitogen-activated protein kinase kinase 2 82.13% 80.00%
CHEMBL2413 P32246 C-C chemokine receptor type 1 81.80% 89.50%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 81.54% 96.47%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.47% 89.00%
CHEMBL3922 P50579 Methionine aminopeptidase 2 80.46% 97.28%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Scutellaria alpina

Cross-Links

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PubChem 162904760
LOTUS LTS0048231
wikiData Q104917124